Associate Manufacturing

Amgen; West Greenwich (RI); On-site; USD 60,000 - 95,000; Full time

Job summary

Amgen is hiring for an Associate Manufacturing - Days (A Shift) to perform manufacturing operations in the Buffer and Media area. You will follow SOPs, run processes, draft documents, and support cross-functional teams.

The role supports continuous improvements and troubleshooting within a fast-paced biotech environment. The position emphasizes compliance with GMP, CFRs, and documentation standards, with opportunities to contribute to a patient-centered mission.

Qualifications

• High school/GED with manufacturing/operations experience or an Associate’s + 6 months of experience or a Bachelor’s degree.
• Knowledge of large-scale Buffer and Media operations and GMP processing.
• Awareness of CFR/regulatory requirements.
• Mechanical ability and troubleshooting experience.
• LIMS access and basic lab equipment familiarity.
• Basic statistical/math skills and GMP interpretation.
• Technical writing capability with TrackWise access.
• Ability to collaborate with cross-functional teams.
• Understanding of chemistry, biology, and physical principles.
• Hands-on experience with Buffer/Media equipment troubleshooting.

Responsibilities

• Perform operations in Buffer and Media processes following SOPs.
• Execute routine validation protocols and draft/ revise documents (Mfg Procedures, SOPs, reports).
• Review documentation for assigned functions and assist in deviations.
• Participate on cross-functional teams and support Solutions Prep.
• Identify, recommend, and implement improvements to routine functions.

Skills

GMP knowledge

Technical writing

Troubleshooting

Team collaboration

Statistical skills

Process improvement

Documentation review

Education

High school diploma or GED

Associate’s degree

Bachelor’s degree

Tools

DeltaV

LIMS

Job description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Associate Manufacturing - Days (A Shift)

What You Will Do

Let’s do this. Let’s change the world. In this vital role you will perform operations in the Manufacturing area, specifically Buffer and Media processes. Operations will be performed according to Standard Operating Procedures (SOPs). Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams and represent the Solutions Prep group. Associate may also have the responsibility of owning minor deviations. In addition, Associate may identify, recommend, and implement improvements related to routine functions.

What We Expect Of You

We are all different, yet we all use our outstanding contributions to serve patients. The hard-working professional we seek is a committed team player with these qualifications.

Basic Qualifications:

• High school/GED + 2 years of manufacturing or operations work experience OR
• Associate’s + 6 months of manufacturing or operations work experience OR
• Bachelor’s

Preferred Qualifications:

• Knowledge of large-scale Buffer and Media operations, GMP processing, etc.
• CFR and Regulatory knowledge
• Mechanical ability/expertise
• Knowledge of WIP lab equipment and computers, with LIMS access
• Basic statistical mathematical skills
• Ability to interpret and apply GMP knowledge
• Ability to demonstrate technical writing capability with Trackwise access
• Independently collaborate with support groups.
• Ability to understand, apply and evaluate basic chemistry, biology and physical principles
• Basic troubleshooting skills on Buffer and Media equipment
• Experience with Delta V.
• Experience with lab equipment/testing

What You Can Expect Of Us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.